DSM Biomedical Dental Bone Graft Plus— 510(k) K193212

Name: FDA 510(k) clearance K193212
Creator: U.S. Food and Drug Administration
Published: 2020-09-10

Substantially Equivalent

Dsm Biomedical

FDA 510(k) clearance K193212 for DSM Biomedical Dental Bone Graft Plus, Substantially Equivalent on 2020-09-10. Applicant: Dsm Biomedical. Device class: 2.

Clearance details

Applicant: Dsm Biomedical
Product code: Code NPM
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 2019-11-21
Decision date: 2020-09-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Exton, PA, US

Download summary PDF View on FDA.gov ↗

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